Visitor Monitoring Drug History: LAMPRENE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: LAMPRENE
FDA Application No: (NDA) 019500
Active Ingredient(s): CLOFAZIMINE
Company: NOVARTIS
 
Label History
 
View the label approved on June 22, 2003 for LAMPRENE, (NDA) 019500


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/11/2003 010Labeling Revision Letter
Label 
4/12/2002 009Manufacturing Change or Addition  
6/20/2001 008Manufacturing Change or Addition  
7/13/2000 007Manufacturing Change or Addition  
1/16/1998 006Control Supplement  
9/12/1995 005Manufacturing Change or Addition  
9/5/1995 004Formulation Revision  
7/20/1995 003Control Supplement  
3/30/1989 002Labeling Revision  
9/22/1988 001Control Supplement  
12/15/1986 000Approval  
 
There are no Therapeutic Equivalents
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